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bioRxivBiochemistryPreprint

Discovery of Chirally-dependent Protein O-2-Hydroxyglutarylation by D2HG and L2HG

Zheng ZhangiD, Yi‐Kai LiuiD, Zhuojun LuoiD, Meng‐Ju WuiD, Claudia N. EvansiD, Zihan QuiD, Fanglei XueiD, Zhong‐Yin ZhangiD, Elizabeth I. ParkinsoniD, Nabeel M. BardeesyiD, W. Andy TaoiD

PDFDOI

Abstract

Mutations in isocitrate dehydrogenase 1 (IDH1) and IDH2 are common in multiple types of human cancer, leading to the accumulation of D-2-hydroxyglutarate (D2HG) and the promotion of tumorigenesis1. Here we discovered a novel O-2- hydroxyglutarylation by D2HG using chemical proteomics and further revealed distinct chiral preferences for D/L2HG modifications. Notably, we identified two kinases, MRCKA and SLK, modified by D2HG and L2HG respectively, and detected reduced phosphorylation of their substrates, suggesting an inhibitory effect of D/L 2HG modifications on the kinases activity.

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